Canonical Allele Identifier: PA645481982
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 255361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val890Leu
CA8815831
NM_000152.5:c.2668G>C
CA401326682
NM_000152.5:c.2668G>T